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Clinical Trial Coordinator - CTC-L

Thermo Fisher Scientific

Clinical Trial Coordinator - CTC-L

full-timePosted: Jan 12, 2026

Job Description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Qualifications:

  • Education and Experience: High / Secondary school diploma or equivalent and relevant formal academic / vocational qualification.
  • Bachelor's degree preferred.
  • Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0 to 1 year).
  • In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.


Knowledge, Skills and Abilities:

  • Ability to work in a team or independently as required 􀀀Good organizational skills and strong attention to detail, with proven ability to handle multiple tasks efficiently and effectively 􀀀Demonstrated ability to effectively analyze project-specific data/systems to ensure accuracy and efficiency Strong customer focus 􀀀Flexibility to reprioritize workload to meet changing project timelines
  • Demonstrated ability to attain and maintain a good working knowledge of applicable Country Regulations, ICH Good Clinical
  • Practices, and organization/Client SOPs and WPDs for all non-clinical/clinical aspects of project implementation, execution and closeout
  • Good English language and grammar skills and proficient local language skills as needed 􀀀Good computer skills, proficient in MS Office (Word, Excel, and PowerPoint) and ability to obtain knowledge and master all clinical trial database systems
  • Ability to successfully complete the organizations clinical training program 􀀀Self-motivated, positive attitude and good interpersonal skills
  • Effective oral and written communication skills
  • Good interpersonal skills
  • Essential judgment and decision-making skills
  • Capable of accurately following project work instructions
  • Good negotiation skills
  • Independent thinker
  • Ability to manage risk and perform risk escalation appropriately. ​

Locations

  • Remote, São Paulo, Brazil (Remote)

Salary

Estimated Salary Rangemedium confidence

50,000 - 90,000 USD / yearly

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • Ability to work in a team or independentlyintermediate
  • Good organizational skills and strong attention to detailintermediate
  • Ability to handle multiple tasks efficientlyintermediate
  • Ability to analyze project-specific data/systemsintermediate
  • Strong customer focusintermediate
  • Flexibility to reprioritize workloadintermediate
  • Knowledge of Country Regulations, ICH Good Clinical Practices, and SOPsintermediate
  • Good English language and grammar skillsintermediate
  • Proficient in MS Office (Word, Excel, PowerPoint)intermediate
  • Ability to master clinical trial database systemsintermediate
  • Self-motivated, positive attitudeintermediate
  • Good interpersonal skillsintermediate
  • Effective oral and written communication skillsintermediate
  • Essential judgment and decision-making skillsintermediate
  • Good negotiation skillsintermediate
  • Independent thinkerintermediate
  • Ability to manage risk and perform risk escalationintermediate

Required Qualifications

  • High / Secondary school diploma or equivalent and relevant formal academic / vocational qualification (experience)
  • Bachelor's degree preferred (experience)
  • Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0 to 1 year) (experience)
  • Equivalency of appropriate education, training and/or directly related experience (experience)

Responsibilities

  • Attain and maintain knowledge of regulations and SOPs for project implementation, execution and closeout
  • Successfully complete the organization's clinical training program
  • Accurately follow project work instructions

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Thermo Fisher Scientific logo

Clinical Trial Coordinator - CTC-L

Thermo Fisher Scientific

Clinical Trial Coordinator - CTC-L

full-timePosted: Jan 12, 2026

Job Description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Qualifications:

  • Education and Experience: High / Secondary school diploma or equivalent and relevant formal academic / vocational qualification.
  • Bachelor's degree preferred.
  • Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0 to 1 year).
  • In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.


Knowledge, Skills and Abilities:

  • Ability to work in a team or independently as required 􀀀Good organizational skills and strong attention to detail, with proven ability to handle multiple tasks efficiently and effectively 􀀀Demonstrated ability to effectively analyze project-specific data/systems to ensure accuracy and efficiency Strong customer focus 􀀀Flexibility to reprioritize workload to meet changing project timelines
  • Demonstrated ability to attain and maintain a good working knowledge of applicable Country Regulations, ICH Good Clinical
  • Practices, and organization/Client SOPs and WPDs for all non-clinical/clinical aspects of project implementation, execution and closeout
  • Good English language and grammar skills and proficient local language skills as needed 􀀀Good computer skills, proficient in MS Office (Word, Excel, and PowerPoint) and ability to obtain knowledge and master all clinical trial database systems
  • Ability to successfully complete the organizations clinical training program 􀀀Self-motivated, positive attitude and good interpersonal skills
  • Effective oral and written communication skills
  • Good interpersonal skills
  • Essential judgment and decision-making skills
  • Capable of accurately following project work instructions
  • Good negotiation skills
  • Independent thinker
  • Ability to manage risk and perform risk escalation appropriately. ​

Locations

  • Remote, São Paulo, Brazil (Remote)

Salary

Estimated Salary Rangemedium confidence

50,000 - 90,000 USD / yearly

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • Ability to work in a team or independentlyintermediate
  • Good organizational skills and strong attention to detailintermediate
  • Ability to handle multiple tasks efficientlyintermediate
  • Ability to analyze project-specific data/systemsintermediate
  • Strong customer focusintermediate
  • Flexibility to reprioritize workloadintermediate
  • Knowledge of Country Regulations, ICH Good Clinical Practices, and SOPsintermediate
  • Good English language and grammar skillsintermediate
  • Proficient in MS Office (Word, Excel, PowerPoint)intermediate
  • Ability to master clinical trial database systemsintermediate
  • Self-motivated, positive attitudeintermediate
  • Good interpersonal skillsintermediate
  • Effective oral and written communication skillsintermediate
  • Essential judgment and decision-making skillsintermediate
  • Good negotiation skillsintermediate
  • Independent thinkerintermediate
  • Ability to manage risk and perform risk escalationintermediate

Required Qualifications

  • High / Secondary school diploma or equivalent and relevant formal academic / vocational qualification (experience)
  • Bachelor's degree preferred (experience)
  • Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0 to 1 year) (experience)
  • Equivalency of appropriate education, training and/or directly related experience (experience)

Responsibilities

  • Attain and maintain knowledge of regulations and SOPs for project implementation, execution and closeout
  • Successfully complete the organization's clinical training program
  • Accurately follow project work instructions

Target Your Resume for "Clinical Trial Coordinator - CTC-L" , Thermo Fisher Scientific

Get personalized recommendations to optimize your resume specifically for Clinical Trial Coordinator - CTC-L. Takes only 15 seconds!

AI-powered keyword optimization
Skills matching & gap analysis
Experience alignment suggestions

Check Your ATS Score for "Clinical Trial Coordinator - CTC-L" , Thermo Fisher Scientific

Find out how well your resume matches this job's requirements. Get comprehensive analysis including ATS compatibility, keyword matching, skill gaps, and personalized recommendations.

ATS compatibility check
Keyword optimization analysis
Skill matching & gap identification
Format & readability score
Quiz Challenge

Answer 10 quick questions to check your fit for Clinical Trial Coordinator - CTC-L @ Thermo Fisher Scientific.

10 Questions
~2 Minutes
Instant Score

Related Books and Jobs

No related jobs found at the moment.